Method of making a lactococcal bacteriocin

Abstract

A method of making a bacteriocin produced by Lactococcus lactis NRRL-B-18535 is described. The bacteriocin is useful in foods and other materials and has a wide spectrum of activity against Gram-positive bacteria in a pH range between 2 and 8.

Description

BACKGROUND OF THE INVENTION

(1) Field of the Invention

The present invention relates to a novel bacteriocin derived from a Lactococcus and method of use to inhibit bacteria, particularly in foods and other materials in need of protection from the bacteria. The present invention particularly relates to a bacteriocin produced by Lactococcus lactis LL-1 deposited as NRRL-B-18535 (previously known as Streptococcus lactis).

(2) Prior Art

The lactic streptococci have been previously described to produce a variety of polypeptide antibiotics, diplococcin, lactostrepcins and bacteriocins (Klaenhammer, T. R., Biochemie 70:337-349 (1988)). The term nisin describes a family of polypeptide antibiotics produced by Lactococcus lactis that prevents the outgrowth of Clostridium and Bacillus spores (Eapen, K. C., et al., J. Food. Sci. Technol. 20: 231-240 (1983)). Bacteriocins are also produced by pediococci.

Diplococcin is an antimicrobial agent produced by Lactococcus cremoris. This inhibitor does not inhibit sporeformers and is only active against other dairy lactococci (Davey, G. P. and B. C. Richardson., Appl. Environ. Microbiol. 41:84-89 (1981)). Lactostrepcins are inhibitory proteins produced by the lactococci that inhibit other streptococci. These molecules are active at relatively low pH and activity is completely lost when the pH is raised to 7.0 (Kozak, W., et al., J. Dairy Res. 45:247-257 (1978)).

Bacteriocins produced by lactic lactococci have been observed in many commercial strains (Geis, A., et al., Appl. Environ. Microbiol. 45:205-211 (1983)). Eight bacteriocin types (I-VIII) have been identified on the basis of their activity spectrum, proteolytic enzyme susceptibility, heat stability and cross-reaction with other bacteriocin producers (Geis, A., et al. Appl. Environ. Microbiol. 45:205-211 (1983))

The problem is that the bacteriocins are not active over a wide pH range. It would be very desirable to provide a bacteriocin which is useful in a wide variety of foods regardless of whether they are acidic or basic.

OBJECTS

It is therefore an object of the present invention to provide a novel bacteriocin which is effective at a pH between pH 2 and 8. It is further an object of the present invention to provide a bacteriocin which can be relatively easily isolated from a particular strain of Lactococcus lactis. These and other objects will become increasingly apparent by reference to the following description and the drawings.

IN THE DRAWINGS

FIG. 1 is a high pressure liquid chromatographic (HPLC) amino acid profile of the bacteriocin of the present invention.

GENERAL DESCRIPTION

The present invention relates to a bacteriocin produced by a Lactococcus which comprises: a protein having a molecular weight of about 6000 daltons, which is inactivated by protease and not inactivated by alpha-chymotrypsin, trypsin, lipase, pepsin and lysozyme, inhibits the growth of bacteria selected from the group consisting of Staphylococcus aureus, Staphylococcus epidermidis, Staphylococcus carnosus, Pediococcus pentosaceus, Pediococcus acidilactici, Lactococcus cremoris, Lactococcus lactis, Leuconostoc mesenteroides, Lactobacillus bulgaricus, Lactobacillus fermentum, Lactobacillus bifermentans, Lactobacillus plantarum and Listeria monocytogenes and has an optimal pH for inhibition between about pH 2 and 8.

Further the present invention relates to a method for inhibiting Gram-positive bacteria which can occur with a material which comprises: providing a bacteriocin with the material in an effective amount which inhibits the Gram-positive bacteria, wherein the bacteriocin is derived from a Lactococcus lactis and wherein the bacteriocin is a protein having a molecular weight of about 6000 daltons, is inactivated by protease and not inactivated by alpha-chymotrypsin, trypsin, lipase, pepsin and lysozyme, inhibits the growth of bacteria selected from the group consisting of Staphylococcus aureus, Staphylococcus epidermidis, Staphylococcus carnosus, Pediococcus pentosaceus, Pediococcus acidilactici, Lactococcus cremoris, Lactococcus lactis, Leuconostoc mesenteroides, Lactobacillus bulgaricus, Lactobacillus fermentum, Lactobacillus bifermentans, Lactobacillus plantarum and Listeria monocytogenes and has an optimal pH for inhibition between about pH 2 and 8.

Further the present invention relates to a composition which comprises: an unspoiled food system which is spoiled by Gram-positive bacteria and a bacteriocin derived from cells of a Lactococcus lactis, wherein the composition contains an amount of the bacteriocin to provide between about 10 and 100,000 AU of the bacteriocin per gram of the food system sufficient for the bacteriocin to inhibit the Gram-positive bacteria and wherein the bacteriocin is a protein having a molecular weight of about 6000 daltons, is inactivated by protease and not inactivated by alpha-chymotrypsin, trypsin, lipase, pepsin and lysozyme, inhibits the growth of bacteria selected from the group consisting of Staphylococcus aureus, Staphylococcus epidermidis, Staphylococcus carnosus, Pediococcus pentosaceus, Pediococcus acidilactici, Lactococcus cremoris, Lactococcus lactis, Leuconostoc mesenteroides, Lactobacillus bulgaricus, Lactobacillus fermentum, Lactobacillus bifermentans, Lactobacillus plantarum and Listeria monocytogenes and has an optimal pH for inhibition between about pH 2 and 8.

Further, the present invention relates to a device which comprises: a material on the device which can become infected with Gram-positive bacteria, and a bacteriocin provided with the material in an amount sufficient to inhibit the Gram-positive bacteria, wherein the bacteriocin is from cells of a Lactococcus lactis and is a protein having a molecular weight of about 6000 daltons, is inactivated by protease and not inactivated by alpha-chymotrypsin, trypsin, lipase, pepsin and lysozyme, inhibits the growth of Staphylococcus aureus, Staphylococcus epidermidis, Staphylococcus carnosus, Pediococcus pentosaceus, Pediococcus acidilactici, Lactococcus cremoris, Lactococcus lactis, Leuconostoc mesenteroides, Lactobacillus bulgaricus, Lactobacillus fermentum, Lactobacillus bifermentans, Lactobacillus plantarum and Listeria monocytogenes and has an optimal pH for inhibition between about pH 2 and 8.

Further, the present invention relates to a method for producing a bacteriocin which comprises: incubating live cells of a Lactococcus lactis in a growth medium for the cells so as to produce the bacteriocin in the growth medium, and wherein the bacteriocin is a protein having a molecular weight of about 6000 daltons, is inactivated by protease and not inactivated by alpha-chymotrypsin, trypsin, lipase, pepsin and lysozyme, inhibits the growth of bacteria selected from the group consisting of Staphylococcus aureus, Staphylococcus epidermidis, Staphylococcus carnosus, Pediococcus pentosaceus, Pediococcus acidilactici, Lactococcus cremoris, Lactococcus lactis, Leuconostoc mesenteroides, Lactobacillus bulgaricus, Lactobacillus fermentum, Lactobacillus bifermentans, Lactobacillus plantarum and Listeria monocytogenes and has an optimal pH for inhibition between about pH 2 and 8.

The strain Lactococcus lactis LLA 1.0 has been deposited under the Budapest Treaty with the Northern Regional Research Laboratory in Peoria, Ill. as NRRL-B-18535. It is available only upon request by name and deposit number. The strain has the following fermentation characteristics: it is able to ferment dextrose, mannitol, sucrose, maltose, salicin, rhamnose, trehalose, cellobiose, mannose, fructose and N-acetylglucosamine.

The strain had three resident plasmids measuring about 33.42, 28.57 and 5.82 Mdal in size.

SPECIFIC DESCRIPTION

The following Examples show the production of the bacteriocin from Lactococcus lactis NRRL-B-18535 and its use in foods and other materials. It also shows the amino acid profile of a hydrolyzate of the bacteriocin. The determination of the approximate molecular weight is also shown.

Example 1

Production of the Bacteriocin

Bacterial Strains and Media. The bacterial strains used in this study were routinely grown on MRS Lactobacillus broth (Difco, Detroit, Mich.). Bacteriocin assay. Production of bacteriocin was assayed by spotting cells on MRS agar (Difco Laboratories, Detroit, Mich.) that contained 2.0% MES (�N-morpholino! ethanesulfonic acid buffer; Sigma, St. Louis, Mo.). These plates were incubated at 35.degree. C. for 18 hours. Assay plates were exposed to chloroform vapor for 30 minutes and overlaid with soft agar (0.075%) seeded with indicator cells. Plates were incubated at 32.degree. C. for 18 hours. Isolates producing a clear zone were considered as producing bacteriocin. Inhibitory spectrum of LL-1. The plate assay system was used to evaluate the spectrum of bacteriocin activity. The strain NRRL-B-18535 showed activity against strains of Staphylococcus aureus, S. epidermidis, S. carnosus, Pediococcus pentosaceus, P. acidilactici, Lactococcus cremoris, Lactococcus lactis, Lactobacillus fermentum, Lactobacillus bifermentans, Leuconostoc mesenteroides, Lactobacillus bulgaricus, L. plantarum. Strains of Streptococcus mutans, S. sanguis, S. faecalis and Listeria monocytogenes were not sensitive in this test. The strain NRRL-B-18535 was resistant to nisin.

Example 2

Isolation of Bacteriocin

To produce the bacteriocin, 500 ml of MRS broth (Difco) was inoculated at 1% with an 8 hour old culture of LLA 1.0 grown in MRS broth (Difco, Detroit, Mich.) and was incubated statically at 32.degree. C. for 24 hours. After 24 hours the cells were removed by centrifugation at 16,000.times.g for 20 minutes at 4.degree. C. The supernatant was filtered through a 0.22 micron (pore size) filter (Millipore Corp. Bedford, Mass.). The supernatant was assayed for bacteriocin activity by spotting 5 microliters of this supernatant material onto various media overlaid with soft agar seeded with different indicator cells. These assay plates were incubated at 35.degree. C. or 32.degree. C., respectively. After 24 hours the plates were examined, clear zones associated with the spot were recorded as positive (growth inhibition) and negative (no growth inhibition). The results are shown in Table 1.

TABLE 1______________________________________Inhibition of various bacterial genera with filtersterilized supernatant (LL-1 broth).sup.1______________________________________Listeria monocytogenes +Staphylococcus aureus +Staphylococcus epidermis +Staphylococcus carnosus +Pediococcus acidilactici +Pediococcus pentosaceus +Lactococcus cremoris +Lactococcus lactis +Leuconostoc mesenteroides +Lactobacillus bulgaricus +Lactobacillus casei +Lactobacillus fermentum +Lactobacillus bifermentans +Lactobacillus plantarum +Streptococcus mutans +______________________________________ .sup.1 Titer of LL1 activity is 1600 AU/ml using Pediococcus pentosaceus FBB63C as an indicator strain.

It was particularly surprising that LL-1 was active against Listeria monocytogenes as a crude filter sterilized broth or dried powder from the broth since nisin is not effective against this bacterium unless it is purified.

Example 3

Purification and Characterization of the Bacteriocin

One liter of MRS broth (Difco) was inoculated at 1% with an 8 hour old culture of LLA 1.0 grown in the medium of Example 1 and was incubated statically at 32.degree. C. for 24 hours. After 24 hours the cells were removed by centrifugation at 16,000.times.g for 20 minutes at 4.degree. C. The supernatant was filtered through a 0.22 micron (pore size) filter (Millipore Corp., Bedford, Mass.). The supernatant was assayed for bacteriocin activity by spotting 5 microliters of a serial two-fold dilution series onto MRS plates overlaid with soft agar seeded with indicator cells. Assay plates were incubated at 35.degree. C. The indicator strain was Pediococcus pentosaceus FBB63C. One arbitrary unit (AU) of bacteriocin was defined as 5 microliters of the highest dilution of culture supernatant yielding a definite zone of growth inhibition on the indicator lawn. The titer was expressed as the reciprocal of the highest dilution showing inhibition.

Ammonium sulfate (Sigma Chemical Co., St. Louis, Mo.) was added to the filtered supernatant to 50% (wt/vol) saturation at 4.degree. C. After precipitation for 18 hours at 4.degree. C., the mixture was centrifuged at 16,000.times.g for 15 minutes at 4.degree. C. The precipitate was reconstituted in 25 ml of 0.05M sodium citrate buffer, pH 6.0. The reconstituted precipitate was dialyzed against the 0.05M sodium citrate buffer at 4.degree. C. by using Spectra/Por no. 6 membrane tubing (Spectrum Medical Industries, Inc., Los Angeles, Calif.) and the titer of its activity was determined. The reconstituted dialyzed precipitate was then subjected to further purification with gel filtration chromatographs using Spectra/Gel AcA202 (Spectrum Medical Industries, Inc., Los Angeles, Calif.).

The bacteriocin preparation (6 ml) was applied to an ascending Spectra/Gel AcA 202 column (2.6 by 30 cm) in 0.05M sodium citrate buffer (pH 6.0). Fractions were collected (4 ml) and assayed for bacteriocin activity. The active factors were then collected and concentrated 10-fold in the dialysis tubing by the removal of water with Carbowax 20 (Fisher Scientific Co., Pittsburgh, Pa.). This active concentrated fraction was then applied to an ascending Spectra/Gel AcA 202 column (1.6 by 60 cm) in 0.05M sodium citrate buffer (pH 6.0). The titer of the partially purified bacteriocin was determined and was used for partial characterization of the bacteriocin.

Effects of heat treatment and enzymes. A partially purified sample of bacteriocin LL-1 (6,400 AU/ml) was assayed for thermostability and enzymatic effects on activity. The bacteriocin was incubated with each enzyme at a final concentration of 50 micrograms/ml for 60 minutes. Incubation in the presence of alpha-chymotrypsin and trypsin was at 25.degree. C., and all other enzyme-bacteriocin mixtures were incubated at 37.degree. C. Inactivation of the enzymes was achieved by boiling them for 3 minutes. It is considered to be a type VI bacteriocin because the strain that produces it is resistant to nisin and does not inhibit S. sanguis. Temperature stability of the bacteriocin was assessed by heating a solution of bacteriocin to 80.degree. C. for 60 minutes, 100.degree. C. for 10 minutes, and 121.degree. C. for 15 minutes. After each treatment, bacteriocin samples were assayed for activity. Enzymes. All enzymes were obtained from Sigma. Alpha-chymotrypsin (type II; 47 U/mg) and lipase (type 1; 8.6 U/mg) were dissolved in 0.05M Tris hydrochloride (pH 8.0) containing 0.01M CaCl.sub.2 ; protease (type V; 1 U/mg), lysozyme (grade I, 41,400 U/mg) and trypsin (type IX; 15,000 U/mg) were dissolved in 0.05M Tris hydrochloride (pH 8.0); and pepsin (3,200 U/mg) was dissolved in 0.2M citrate buffer (pH 6.0). pH stability of activity. Partially purified bacteriocin (1 ml) was dialyzed against buffers of various pH's. The bacteriocin solution (12,800 AU/ml) was dialyzed for 18 hours with 2 changes against 0.05M glycine hydrochloride buffer (pH 2.0), 0.05M citrate buffer (pH 3 to 6), 0.05M Tris hydrochloride (pH 7 to 9), and 0.05M carbonate-bicarbonate buffer (pH 10 to 11). After dialysis, the contents of the tubing were assayed for bacteriocin activity. The bacteriocin LL-1 was sensitive to protease and not sensitive to alpha-chymotrypsin, trypsin, lipase, pepsin or lysozyme. The bacteriocin was observed to be most stable from pH 2-8, with some loss in activity at pH 9 and 10. Approximately one-fourth of the activity was still present at pH 11.0. Exposure of the bacteriocin to 121.degree. C. did destroy all of the LL-1 activity. Boiling at 100.degree. C. for 10 minutes resulted in 75% loss in activity of the bacteriocin. This 75% activity loss was also observed at 80.degree. C. for 60 minutes.

Example 4

Nutritional Studies

Each of the media listed in Table 2 was prepared in 100 ml quantities.

The media were adjusted to pH 6.8 before autoclaving. The media were inoculated with an 8 hour culture of NRRL-B-18535 at a rate of 1% and then incubated at 32.degree. C. for 24 hours. After 24 hours, 25 ml of the above culture was centrifuged at 24,000.times.g for 15 minutes at 4.degree. C. The supernatant was then filter sterilized using a 0.22 micron filter (Millipore, Bedford, Mass.) and tested for the least titer which inhibited Pediococcus pentosaceus FBB63C as the indicator strain.

The results of the nutritional study are depicted in Table 2.

TABLE 2______________________________________Nutritional Studies of NRRL-B-18535 for the Productionof Bacteriocin LL-1.Media Titer______________________________________Brain Heart Infusion Broth 0(Difco, Detroit, MI)Tryptic Soy Broth 0(Difco, Detroit, MI)All Purpose Tween Broth 1:2+(Difco, Detroit, MI)MRS Lactobacillus Broth 1:8(Difco, Detroit, MI)MRS + 1% yeast extract 1:4+(Oxoid, Basingstoke, England)MRS + 1% Hy-Soy .TM. 1:8(Sheffield Products, Norwich, NY)MRS + 1% Hy-Case .TM. 1:8(Sheffield Products, Norwich, NY)10% peptonized milk with 01% glucose10% peptonized whey with 01% glucoseCorn Steep Base (I)4% cornsteep3% yeast extract5% glucose with:(a) Nothing 1+(b) 1% N-Z Amine Type AS .TM. 1+ (Sheffield Products, Norwich, NY)(c) 1% PRIMATONE SGM .TM. 1+ (Sheffield Products, Norwich, NY)(d) 1% EDAMIN K .TM. 1 (Sheffield Products, Norwich, NY)(e) 1% PRIMAGEN P .TM. 1:2 (Sheffield Products, Norwich, NY)(f) 1% PRIMATONE HS .TM. 1:2 (Sheffield Products, Norwich, NY)(g) 1% EDAMIN S .TM. 1+ (Sheffield Products, Norwich, NY)(h) 1% AMICASE T .TM. 1:2 (Sheffield Products, Norwich, NY)(i) 1% AMICASE .TM. 1:2 (Sheffield Products, Norwich, NY)(j) 1% PRIMATONE .TM. 1:2 (Sheffield Products, Norwich, NY)(k) 1% AMISOY .TM. 1:2+ (Sheffield Products, Norwich, NY)(l) 1% HYSOY TYPE T .TM. 1 (Sheffield Products, Norwich, NY)(m) 1% PRIMATONE G .TM. 1:2 (Sheffield Products, Norwich, NY)(n) 1% PRIMAGEN .TM. 1:2+ (Sheffield Products, Norwich, NY)CORN STEEP BASE (II)4% cornsteep5% dextrose, with:(a) 2% AMISOY .TM. 1:2(B) 2% primagen .TM.______________________________________ The most effective medium for the production of bacteriocin LL-1 appears to be MRS broth that is unsupplemented. Other media were not as effective and protein hydrolysate supplements did not stimulate bacteriocin production. Whey or milk based media were the least effective for the production of LL-1.

Example 5

Production of Dried Bacteriocin LL-1

Lactococcus lactis NRRL-B-18535 was grown in one liter of MRS broth (Difco, Detroit, Mich.) for 24 hours at 32.degree. C. The cells were pelleted by centrifugation at 16,000.times.g at 4.degree. C., and the supernatant was collected. The supernatant was then filter sterilized with a 0.22 micron pore size filter. Nonfat dry milk powder was added to 10% (weight/volume) to facilitate drying. This mixture was lyophilized into a dry powder.

Example 6

Minimum inhibitor concentration (MIC) of the lyophilized bacteriocin LL-1 against Pediococcus pentosaceus FBB63c

The bacteriocin LL-1 powder of Example 5 was dissolved in APT broth or Tryptic Soy Broth and two-fold serially diluted to concentrations ranging from 1000 AU/ml to 2.0 AU/ml. Approximately 1.times.10.sup.3 Pediococcus pentosaceus/ml were added to each of the tubes which were then incubated for 24 hours at 35.degree. C. The MIC value was the lowest concentration tube displaying no visible turbidity. The results are summarized in Table 3.

TABLE 3______________________________________Strain MIC______________________________________Pediococcus pentosaceus 8.0 AU/ml______________________________________

Example 7

Minimum inhibitory concentration (MIC) of the lyophilized bacteriocin LL-1 against Staphylococcus aureus 265

The bacteriocin LL-1 powder of Example 5 was dissolved in APT broth or Tryptic Soy Broth and two-fold serially diluted to concentrations ranging from 1000 AU/ml to 2.0 AU/ml. Approximately 1.times.10.sup.3 Staphylococcus aureus/ml were added to each of the tubes which were then incubated for 24 hours at 35.degree. C. The MIC value was the lowest concentration tube displaying no visible turbidity. The results are summarized in Table 4.

TABLE 4______________________________________Strain MIC______________________________________Staphylococcus aureus 1000 AU/ml______________________________________

Example 8

LL-1 prepared as in Examples 2, 3 and 4 (1600 AU/ml) is highly effective against Listeria monocytogenes as a crude filter sterilized broth (or powder derived therefrom), whereas nisin must be at least semi-purified from the broth concentrated to be significantly effective. This is shown by the following data in Table 5.

TABLE 5______________________________________ LL-1.sup.(1) NISIN.sup.(2) 1600 AU/ml 370 IU/ml______________________________________L. monocytogenes 69 + -______________________________________ + = Inhibition - = No inhibition .sup.(1) 1,600 AU/ml of LL1 is 0.016 mg of pure LL1 directly from the broth after being filter sterilized. .sup.(2) 370 IU of nisin is 0.01 mg pure nisin which has been purified from the broth. The practical result is that lyophilized, filter sterilized LL-1 is easier and less expensive to prepare than nisin because subsequent purification after filter sterilization is not required.

Example 9

Molecular weight determination of the bacteriocin LL-1

The molecular weight of the bacteriocin of Example 3 was determined by gel filtration. 1.5 ml (800 AU/ml) was applied to an ascending Spectra/Gel AcA 202 column (1.6 by 60 cm: Spectrum, Los Angeles, Calif.) in 0.05M sodium citrate buffer (pH 6.0). The elution volume of the bacteriocin was compared to the elution volumes of standard proteins. Bacteriocin activity was determined as described above. The protein standards and their molecular weights included the following: cytochrome C, 12,400; aprotinin, 6,500; melittin, 2,846 (Sigma).

The bacteriocin preparations were examined on 12% SDS-PAGE gel. Samples and molecular weight standards 1 mg/ml were dissolved in sample buffer and loaded on the gel. The material was then subjected to electrophoresis for 1 hour at 16 mA and then for 1 hour at 24 mA. The gel was then stained with silver strain (BioRad, Richmond, Calif.) or assayed for bacteriocin activity by a direct detection system (Bhunia, A. K. et al., Appl. Bacteriol. 65:261-268 (1988)).

The molecular weight was observed to be approximately 6,000 daltons from gel filtration. The SDS gel overlay with Pediococcus pentosaceus confirmed the approximate size observed with gel filtration.

Example 10

Amino acid profile of purified bacteriocin LL-1

The bacteriocin was purified as previously described in Example 9. An active concentrated fraction from the Spectra/Gel AcA 202 column was subjected to further purification using a C-8 analytical column. Fractions were assayed for bacteriocin activity. The active fractions were then further concentrated using the Speed Vac Concentrator.TM. (Savant Instruments Inc. Farmingdale, N.Y.) and resuspended in 50 microliters of distilled water. This material was then analyzed for amino acid content using a modification of the PICO-TAG.TM. system (Waters Associates, Milford, Mass.). The method involves sample hydrolysis followed by derivatization with phenylisothiocyanate and subsequent analysis by HPLC �Mundt, M. O., W. G. Beattie, and F. R. Wieland, J. Bacteriol. 98:938-942 (1969)!. Amino acids were identified by comparing the retention times of a known standard to that of the active fraction hydrolyzate (FIG. 1.). The results listed in Table 6 compare the ratios of the various amino acids observed to glutamic acid, which was observed in the greatest amount.

TABLE 6______________________________________Ratios of various amino acids to glutamic acid.Amino Acid Ratio to glutamic acid______________________________________Aspartic acid 0.42Glutamic acid 1.0Serine 0.35Glycine 0.83Histidine 0.16Arginine 0.35Threonine 0.34Alanine 0.76Proline 0.48Tyrosine 0.19Valine 0.43Methionine 0.14Cysteine 0.12Isoleucine 0.27Leucine 0.64Phenylalanine 0.19Lysine 0.50______________________________________

Example 11

Salad Dressing with Added contaminant Microorganisms

The following Tables 7, 8 and 9 show the use of the bacteriocin LL-1 in salad dressing to which Lactobacillus fermentum NRRL-B-18586 has been added. The spoilage bacterium strain is one which is very active in food spoilage.

TABLE 7______________________________________ Desig- Dres- Spoilage Dilution nation sing.sup.1 Bacteria.sup.2 LL-1.sup.3 Buffer.sup.4______________________________________Uninoculated A 100 g 0 0 3.9 mlControlInoculated B 100 g 0.1 ml (10.sup.6) 0 3.9 mlControlInoculated C 100 g 0.1 ml (10.sup.6) 0.78 ml 3.12 mlplusbacteriocinLL-1 (200 AU/g)Inoculated D 100 g 0.1 ml (10.sup.6) 3.9 ml 0plusbacteriocinLL-1 (1000 AU/g)______________________________________ .sup.1 Dressing used was Marie's .TM. Ranch Dressing. The general composition of the salad dressing was soybean oil, fresh buttermilk, whol eggs, egg yolks, distilled vinegar, sugar, salt, spices, garlic, onion an xanthan gum. .sup.2 Lactobacillus fermentum NRRLB-18586 streptomycin resistant, addition about 3.0 .times. 10.sup.3 cfu/g of salad dressing. .sup.3 Bacteriocin LL1 used was a 50% ammonium sulfate preparation that was dialyzed against 0.05 M sodium citrate buffer (pH 6.), then filter sterilized. (Concentration: 25,600 AU/ml). The experiment was conducted a 25.degree. C. for ten days. .sup.4 The dilution buffer was used to provide equivalent volumes of adde fluid. TABLE 8______________________________________Bacterial Counts in the Salad Dressing. Time (days)Designation T-0.sup.a T-1 T-10______________________________________A <10.sup.2b <10.sup.2 <10.sup.2B 4.0 .times. 10.sup.3 3.1 .times. 10.sup.3 7.0 .times. 10.sup.2C 3.0 .times. 10.sup.3 2.2 .times. 10.sup.3 2.5 .times. 10.sup.2D 2.3 .times. 10.sup.3 3.5 .times. 10.sup.2 <10.sup.2______________________________________ .sup.a Time (days) .sup.b Bacterial Counts (cfu/g) Lactobacillus fermentum 18586 Sm.sup.r TABLE 9______________________________________Organoleptic Evaluation of Salad Dressing. Designation T-10.sup.a______________________________________ A Not spoiled B Spoiled.sup.b C Not spoiled D Not spoiled______________________________________ .sup.a Time (days) .sup.b Acetic acid was detected by smell and taste, and gas (CO.sub.2) wa produced and observed in the dressing as evidence of spoilage.

This Example shows that the bacteriocin LL-1 was effective to inhibit spoilage bacteria introduced into a salad dressing.

Example 12

Salad Dressing With Natural Contaminant Microorganisms

The following Tables 10 and 11 demonstrate the inhibition of the normal, lactic acid spoilage flora using the bacteriocin LL-1 in salad dressing:

TABLE 10______________________________________ Desig- Dilution nation Dressing.sup.1 LL-1.sup.2 Buffer______________________________________Uninoculated A 100 g 0 3.9 mlControlUninoculated B 100 g 0.78 ml 3.12 mlplus bacteriocinLL-1 (200 AU/g)Uninoculated plus C 100 g 3.9 ml 0bacteriocinLL-1 (1000 AU/g)______________________________________ .sup.1 Dressing used was Marie's .TM. Ranch Dressing. The general composition of the salad dressing was soybean oil, fresh buttermilk, whol eggs, egg yolks, distilled vinegar, sugar, salt, spices, garlic, onion an xanthan gum. Because of the natural ingredients there is a high level of lactic bacteria such as Lactabacillus fermentum NRRLB-18586 in the salad dressing. .sup.2 Bacteriocin LL1 used was a 50% ammonium sulfate preparation that was dialyzed against 0.05 M sodium citrate buffer (pH 6.0), then filter sterilized. (Concentration: 25,600 AU/ml). The dilution buffer was used t provide equivalent volumes of added liquid with LL1.

The experiment was conducted at 25.degree. C. for ten days.

TABLE 11______________________________________Bacterial counts in the salad dressing. Time (days)Designation T-0.sup.a T-2 T-20______________________________________A <10.sup.2b <10.sup.3 10.sup.8B 10.sup.2 <10.sup.2 10.sup.5C 10.sup.2 <10.sup.2 10.sup.3______________________________________ .sup.a Time (days) .sup.b Bacterial Counts (cfu/g) Lactobacillus sp. spoilage agents.

The results show that LL-1 was very effective in inhibiting the growth of the lactic bacteria naturally present in the salad dressing.

The bacteriocin LL-1 was stable in various environments. The bacteriocin was effective in reducing the initial contaminant bacteria load and maintaining this protection over a period of several days. The same results can be achieved in various food systems such as gravies, meats, vegetables and the like, which can be raw or cooked, and particularly coleslaw, macaroni salad, potato salad and sausages. The bacteriocin is particularly effective where raw foods are mixed with other ingredients which promote the growth of Gram-positive bacteria naturally present on food. The bacteriocin can be effective on such items as bandages, sanitary napkins and ointments (liquids and powders) used for wound healing. In general, the bacteriocin can also be useful in the form of ointments (liquids, or powders) as disinfectant for animate and inanimate objects where Staphylococcus aureus is a problem. The bacteriocin can also be used to treat wounds in mammals which can be infected with Gram-positive bacteria.

It is intended that the foregoing description be only illustrative of the present invention and that the present invention be limited only by the hereinafter appended claims.

Claims

1. A method for producing a bacteriocin in a growth medium which comprises:

(a) culturing live cells of Lactococcus lactis NRRL-B-18535 in a growth medium for the cells so as to produce the bacteriocin in the growth medium, and wherein the bacteriocin contains a protein having a molecular weight of about 6000 daltons, is inactivated by protease V and not inactivated by alpha-chymotrypsin, trypsin, lipase, pepsin and lysozyme, wherein the bacteriocin inhibits the growth of bacteria selected from the group consisting of Staphylococcus aureus, Staphylococcus epidermidis, Staphylococcus carnosus, Pediococcus pentosaceus, Pediococcus acidilactici, Lactococcus cremoris, Lactococcus lactis, Leuconostoc mesenteroides, Lactobacillus bulgaricus, Lactobacillus fermentum, Lactobacillus bifermentans, Lactobacillus plantarum and Listeria monocytogenes and has an pH for inhibition between about pH 2 and 8; and

(b) separating the bacteriocin in the growth medium from the cells.

2. A method for producing a bacteriocin which comprises:

(a) culturing live cells of Lactococcus lactis NRRL-B-18535 in a growth medium for the cells to produce the bacteriocin;

(b) separating the bacteriocin from the cells; and

(c) isolating the bacteriocin from the growth medium, wherein the bacteriocin contains a protein having a molecular weight of about 6000 daltons, is inactivated by protease V and not inactivated by alpha-chymotrypsin, trypsin, lipase, pepsin and lysozyme, wherein the bacteriocin inhibits the growth of Staphylococcus aureus, Staphylococcus epidermidis, Staphylococcus carnosus, Pediococcus pentosaceus, Pediococcus acidilactici, Lactococcus cremoris, Lactococcus lactis, Leuconostoc mesenteroides, Lactobacillus bulgaricus, Lactobacillus fermentum, Lactobacillus bifermentans, Lactobacillus plantarum and Listeria monocytogenes and has an pH for inhibition between about pH 2 and 8.

3. The method of claim 2 wherein the bacteriocin is lyophilized after isolation from the growth medium.

4. A method for producing a bacteriocin which comprises:

(a) culturing live cells of Lactococcus lactis NRRL-B-18535 in a growth medium for the cells, so as to produce the bacteriocin in the growth medium;

(b) separating bacteriocin from the cells: and

(c) recovering the bacteriocin from the growth medium from the bacterocin by precipitating the bacteriocin in the growth medium and removing the precipitated bacteriocin to provide the bacteriocin, and wherein the bacteriocin contains a protein having a molecular weight of about 6000 daltons, is inactivated by protease V and not inactivated by alpha-chymotrypsin, trypsin, lipase, pepsin and lysozyme, inhibits the growth of bacteria selected from the group consisting of Staphylococcus aureus, Staphylococcus epidermidis, Staphylococcus carnosus, Pediococcus pentosaceus, Pediococcus acidilactici, Lactococcus cremoris, Lactococcus lactis, Leuconostoc mesenteroides, Lactobacillus bulgaricus, Lactobacillus fermentum, Lactobacillus bifermentans, Lactobacillus plantarum and Listeria monocytogenes and has an pH for inhibition between about pH 2 and 8.

5. The method of claim 4 wherein the bacteriocin is lyophilized.

6. The method of claim 4 wherein the bacteriocin partially purified from the growth medium by precipitation using ammonium sulfate and the precipitated bacteriocin is recovered from the growth medium.

7. A method for producing a bacteriocin in the growth medium which comprises:

(a) culturing cells of Lactococcus lactis NRRL-B-18535 in a growth medium for the cells to produce, the bacteriocin in the growth medium;

(b) filtering the cultured growth medium in a microporous filter means so that the bacteriocin can pass through as a filtrate and which retains components of the growth medium and the cells on the filter means to produce the bacteriocin, and wherein the bacteriocin contains a protein having a molecular weight of about 6000 daltons, is inactivated by protease v and not inactivated by alpha-chymotrypsin, trypsin, lipase, pepsin and lysozyme, inhibits the growth of bacteria selected from the group consisting of Staphylococcus aureus, staphylococcus epidermidis, Staphylococcus carnosus, Pediococcus pentosaceus, Pediococcus acidilactici, Lactococcus cremoris, Lactococcus lactis, Leuconostoc mesenteroides, Lactobacillus bulgaricus, Lactobacillus fermentum, Lactobacillus bifermentans, Lactobacillus plantarum and Listeria monocytogenes and has an pH for inhibition between about pH 2 and 8.

8. The method of claim 7 further comprising lyophilizing the filtered bacteriocin.

9. The method of claim 7 wherein the bacteriocin in the filtrate is precipitated with ammonium sulfate and then the precipitated bacteriocin is recovered from the growth medium is further purified by liquid chromatography.